BEGIN:VCALENDAR X-WR-TIMEZONE:US/Eastern DTSTART:20190109T130000 DTEND:20190109T143000 VERSION:2.0 LOCATION:OnlinePRODID:-//Training Doyens //EN METHOD:REQUEST BEGIN:VEVENT UID:20190109T000000-1742955512-example.com DTSTAMP:20190109T000000 DTSTART;TZID="US/Eastern":20190109T130000 DTEND;TZID="US/Eastern":20190109T143000 SUMMARY:Computer System Validation (CSV) for FDA-Regulated Computers DESCRIPTION: FDA requires that all computer systems used to produce, manage and report on GxP (GMP, GLC, GCP) related products be validated and maintained in accordance with FDA system validation rules. You’ll learn all about how to create and maintain good FDA-compliant documentation using a strategic approach based on the System Development Life Cycle (SDLC) Methodology. The webinar will leave you with the information needed for planning, executing and documenting a computer system validation effort that meets FDA compliance standards. You will learn about the computer system validation requirements and what must be done to ensure the system remains in a validated state. In addition, you’ll learn about the various computer system validation deliverables and how to document them through the entire process. PRIORITY:3END:VEVENT END:VCALENDAR